Using Su Jok Therapy to Help Breastfeeding
The Effect of Su Jok Therapy on Breastfeeding Success, Breastfeeding Self-Efficacy and Perception of Insufficient Milk After Caesarean Section in Primiparas
This study is testing if Su Jok therapy can help new mothers who had cesarean sections produce more breast milk while breastfeeding.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 19 Years to 35 Years |
| Sex | Female |
| Sponsor | University of Gaziantep Academic / other |
| Locations | 1 site (Sanliurfa, Eyalet/Yerleşke) |
| Trial ID | NCT06628960 on ClinicalTrials.gov |
What this trial studies
This study investigates the effects of Su Jok therapy, a form of acupressure and acupuncture, on enhancing breastfeeding in primiparous women who have undergone cesarean sections. The therapy involves applying various techniques such as massage, moxa, needles, magnets, and seeds to specific points on the hands and feet, which are believed to correspond to different body systems. The goal is to determine if this alternative therapy can effectively increase breast milk production in new mothers. The study will include women aged 19-35 who are breastfeeding and willing to participate.
Who should consider this trial
Good fit: Ideal candidates for this study are first-time mothers aged 19-35 who have delivered via cesarean section and are currently breastfeeding.
Not a fit: Patients who are not breastfeeding or those who have not undergone a cesarean section may not benefit from this study.
Why it matters
Potential benefit: If successful, this therapy could provide a non-invasive method to enhance breastfeeding for new mothers, potentially improving infant nutrition.
How similar studies have performed: While there is limited literature on Su Jok therapy, no prior studies have specifically examined its effects on increasing breast milk production, making this approach relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * primiparous women giving birth by caesarean section, * women aged 19-35, * breastfeeding women Exclusion Criteria: * those who refused to participate in the research
Where this trial is running
Sanliurfa, Eyalet/Yerleşke
- Şanlıurfa training and research hospital — Sanliurfa, Eyalet/Yerleşke, Turkey (Türkiye) (Recruiting)
Study contacts
- Principal investigator: AYŞEGÜL KILIÇLI, Assisstan. Prof. PhD. — Muş Alparslan University
- Study coordinator: AYŞEGÜL KILIÇLI, Assisstan. Prof. PhD.
- Email: aysegul_ay_9@hotmail.com
- Phone: (0436) 212 06 70
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.